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Value of gadoxetate biliary transit time in determining hepatocyte function
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  • 作者:Jianwei Wu ; Hui Li ; Yuning Lin ; Ziqian Chen ; Qun Zhong ; Hong Gao…
  • 关键词:Magnetic resonance imaging ; Cirrhosis ; Gadoxetate ; Hepatobiliary phase
  • 刊名:Abdominal Imaging
  • 出版年:2015
  • 出版时间:January 2015
  • 年:2015
  • 卷:40
  • 期:1
  • 页码:95-101
  • 全文大小:728 KB
  • 参考文献:1. Hamm B, Staks T, Muhler A, et al. (1995) Phase I clinical evaluation of Gd-EOB-DTPA as a hepatobiliary MR contrast agent: safety, pharmacokinetics, and MR imaging. Radiology 195(3):785-92 CrossRef
    2. Kim H, Kim MJ (2013) Hepatic uptake of gadoxetic acid. Radiology 267(1):314-15 CrossRef
    3. van Montfoort JE, Stieger B, Meijer DK, et al. (1999) Hepatic uptake of the magnetic resonance imaging contrast agent gadoxetate by the organic anion transporting polypeptide Oatp1. J Pharmacol Exp Ther 290(1):153-57
    4. Jang YJ, Cho SH, Bae JH, et al. (2013) Noninvasive assessment of hepatic fibrosis using gadoxetate-disodium-enhanced 3T MRI. Ann Hepatol 12(6):926-34
    5. Schuhmann-Giampieri G, Schmitt-Willich H, Press WR, et al. (1992) Preclinical evaluation of Gd-EOB-DTPA as a contrast agent in MR imaging of the hepatobiliary system. Radiology 183(1):59-4 CrossRef
    6. Hoekstra LT, de Graaf W, Nibourg GA, et al. (2013) Physiological and biochemical basis of clinical liver function tests: a review. Ann Surg 257(1):27-6 CrossRef
    7. Carson ER, Jones EA (1979) Use of kinetic analysis and mathematical modeling in the study of metabolic pathways in vivo: applications to hepatic organic anion metabolism (second of two parts). N Engl J Med 300(19):1078-086 CrossRef
    8. Feier D, Balassy C, Bastati N, et al. (2013) Liver fibrosis: histopathologic and biochemical influences on diagnostic efficacy of hepatobiliary contrast-enhanced MR imaging in staging. Radiology 269(2):460-68 CrossRef
    9. Verloh N, Haimerl M, Rennert J, et al. (2013) Impact of liver cirrhosis on liver enhancement at Gd-EOB-DTPA enhanced MRI at 3 Tesla. Eur J Radiol 82(10):1710-715 CrossRef
    10. Chernyak V, Kim J, Rozenblit AM, Mazzoriol F, Ricci Z (2011) Hepatic enhancement during the hepatobiliary phase after gadoxetate disodium administration in patients with chronic liver disease: the role of laboratory factors. J Magn Reson Imaging 34(2):301-09 CrossRef
    11. Okada M, Ishii K, Numata K, et al. (2012) Can the biliary enhancement of Gd-EOB-DTPA predict the degree of liver function? Hepatobiliary Pancreat Dis Int 11(3):307-13 CrossRef
    12. Yamada A, Hara T, Li F, et al. (2011) Quantitative evaluation of liver function with use of gadoxetate disodium-enhanced MR imaging. Radiology 260(3):727-33 CrossRef
    13. Wibmer A, Aliya Q, Steininger R, et al. (2012) Liver transplantation: impaired biliary excretion of gadoxate is associated with an inferior 1-year retransplantation-free survival. Invest Radiol 47(6):353-58 CrossRef
    14. Wibmer A, Prusa AM, Nolz R, et al. (2013) Liver failure after major liver resection: risk assessment by using preoperative Gadoxetic acid-enhanced 3-T MR imaging. Radiology 269(3):777-86 CrossRef
    15. Cho SH, Kang UR, Kim JD, Han YS, Choi DL (2011) The value of gadoxetate disodium-enhanced MR imaging for predicting posthepatectomy liver failure after major hepatic resection: a preliminary study. Eur J Radiol 80(2):e195–e200 CrossRef
    16. Motosugi U, Ichikawa T, Sou H, et al. (2009) Liver parenchymal enhancement of hepatocyte-phase images in Gd-EOB-DTPA-enhanced MR imaging: which biological markers of the liver function affect the enhancement? J Magn Reson Imaging 30(5):1042-046 CrossRef
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Imaging and Radiology
    Gastroenterology
    Hepatology
  • 出版者:Springer New York
  • ISSN:1432-0509
文摘
Objective To determine if transit time for excretion of gadoxetate into major bile ducts and duodenum correlates with clinical models of hepatocellular function. Methods This retrospective research was approved by the Institutional Review Board with waiver of informed consent. Search of the radiology database from January 1, 2013 to March 4, 2014 revealed 84 patients with chronic liver disease (65 males, mean age 47?years). Eighteen control subjects with no known liver disease or risk factors were also enrolled for analysis (9 males, mean age 43?years). MRI was performed with hepatobiliary phases at 10, 15, 20, and 25?min after injection of 0.025 mmol/kg of gadoxetate (Primovist, Bayer HealthCare, Shanghai, China). The time of excreted contrast appearing in the biliary tree and in the duodenum was recorded. Linear trend analysis was performed to determine the relationship between excretion time and hepatic function. Results The patient cohort was stratified by Child-Pugh classification (A, B, and C with n?=?53, 27, and 4, respectively). Arrival of gadoxetate in the gall bladder at 10-min hepatobiliary phase was seen in 87% of control group and 45% of Child-Pugh A group (p?=?0.02). There was no difference between these groups for later hepatobiliary phases. The arrival of biliary contrast in the right hepatic duct, common bile duct, and gall bladder were significantly earlier in the Child-Pugh A group compared to the Child-Pugh B/C group at all hepatobiliary phases after 10?min (p?p?=?0.01). There was no difference in entry time of gadoxetate into the duodenum between the normal, Child-Pugh A, and Child-Pugh B/C groups. Conclusions The transit time for gadoxetate to appear in extrahepatic duct is a reasonable indicator of liver function, and may be included in radiology reports. The appearance in the duodenum, however, may depend on factors other than liver function, such as the physiology of the gallbladder and sphincter of Oddi.

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